Data / Medical devices / Stimulator, Peripheral Nerve, Implanted (Pain Relief) / United States
FDA-registered makers of Stimulator, Peripheral Nerve, Implanted (Pain Relief) in the United States: 17 establishments
17 establishments in the United States are registered with the FDA to make Stimulator, Peripheral Nerve, Implanted (Pain Relief) (product code GZF). 6 have a 510(k) clearance or PMA approval on file and 2 have a recall event. FDA data exported November 2, 2026.
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- Device
- Stimulator, Peripheral Nerve, Implanted (Pain Relief)
- Product code
- GZF
- Country
- United States
Makers of Stimulator, Peripheral Nerve, Implanted (Pain Relief) in the United States
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Bioventus LLC | Durham, NC, United States | Manufacturer, Specification developer | 6 | July 16, 2025 | 0 | 0 | 0 | api.fda.gov |
| Bioventus LLC | Cordova, TN, United States | Complaint file establishment, Manufacturer | 6 | July 16, 2025 | 0 | 0 | 0 | api.fda.gov |
| Curonix LLC | Pompano Beach, FL, United States | Complaint file establishment, Manufacturer, Specification developer | 3 | June 20, 2024 | 0 | 1 | 0 | api.fda.gov |
| Medtronic Neuromodulation | Minneapolis, MN, United States | Manufacturer | 2 | April 12, 2000 | 0 | 0 | 0 | api.fda.gov |
| Medtronic Puerto Rico Operations Co., Juncos | Juncos, PR, United States | Manufacturer | 2 | April 12, 2000 | 0 | 0 | 0 | api.fda.gov |
| MiniStim Corp | Boca Raton, FL, United States | Manufacturer | 1 | August 14, 2020 | 0 | 0 | 0 | api.fda.gov |
| Abbott Medical | Plano, TX, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Cirtec Medical | Brooklyn Park, MN, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Cirtec Medical | Enfield, CT, United States | Contract manufacturer, Contract sterilizer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Heraeus Medical Components, LLC | Saint Paul, MN, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Medtronic Puerto Rico Operations Co., Villalba | Villalba, PR, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Nalu Medical | Carlsbad, CA, United States | Manufacturer, Specification developer | 0 | 0 | 1 | 0 | api.fda.gov | |
| Pro-Tech Design & MFG., Inc. | Santa Fe Springs, CA, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| PRO-TECH Design & Mfg, Inc. | Santa Fe Springs, CA, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Resolution Medical | Minneapolis, MN, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Spectrum Assembly Inc. | Carlsbad, CA, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Technical Services For Electronics, Inc. | Jackson, MN, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov |
Updated November 2, 2026. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.